Thallim, bismuth and lead containing oxide superconductor

ABSTRACT

Superconducting oxide material containing compound represented by the formula: 
     
         (Tl.sub.(1-p-q) Bi.sub.p Pb.sub.q).sub.y γ.sub.z (α.sub.(1-r) 
    
      β r ) s  Cu v  O w   
     in which each of &#34;α&#34; and &#34;γ&#34; is an element selected in IIa group of the periodic table, &#34;β&#34; is an element selected from a group comprising Na, K, Rb and Cs, &#34;y&#34;, &#34;z&#34;, &#34;v&#34;, &#34;w&#34;, &#34;p&#34;, &#34;q&#34;, &#34;r&#34; and &#34;s&#34; are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦6.0, 1.0≦v, 5.0≦w, 0≦p≦1.0, 0≦q≦1.0, 0≦r≦1.0 and 0.5≦s≦3.0.

This is a Continuation of application Ser. No. 07/852,331, filed Mar. 17, 1992, abandoned, which is a continuation of Ser. No. 436,011, filed Nov. 13, 1989, abandoned.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to superconducting oxide materials and processes for preparing the same. More particularly, it relates to thallium-containing superconducting oxide materials having high superconducting critical temperature (Tc) and higher superconducting critical current density (Jc) and processes for preparing the same.

2. Description of the Related Art

Discovery of new oxide type superconductor by Bednorz and Muller revealed the possibility of high temperature superconductors (Z. Phys. B64, 1986 p 189).

The new type oxide superconductor discovered by Bednorz and Muller is represented by [La, Sr]₂ CuO₄ which is called the K₂ NiF₄ -type oxide having a crystal structure similar to known perovskite type oxides. The K₂ NiF₄ -type compound oxides show such higher Tc as 30 K. which are extremely higher than known superconducting materials.

C. W. Chu et al. reported another superconducting material of so-called YBCO type represented by YBa₂ Cu₃ O_(7-x) having the critical temperature of about 90 K. (Physical Review letters, Vol. 58, No. 9, p 908). However, the critical temperature of this oxide superconductor is not so different from a boiling point 70 K. of liquid nitrogen and hence the other oxide materials which have much higher critical temperature, in other words, which have larger temperature margin have been demanded.

Maeda et al reported the other type new superconducting compound oxide of Bi--Sr--Ca--Cu--O system which show the critical temperature of more than 100 K. (Japanese Journal of Applied Physics. Vol. 27, No. 2, p 1209 to 1210).

Thallium type compound oxides are also high Tc superconductors of more than 100 K. The present inventors disclosed several kinds of thallium type compound oxides superconductors in U.S. Pat. application No. 223,634 filed on Jul. 25, 1988, now U.S. Pat. No. 4,880,773, and Hermann et al. reported Tl--Ba--Ca--Cu--O system in Appl. Phys. Lett. 52 (20) p 1738. U.S. Pat. No. 4,870,052 discloses a kind of thallium-containing oxide superconductor. Thallium type compound oxides have such a very important merit that superconductors which show such a high Tc as more than 100 K. can be obtained without using rear earth elements as a material so that the production cost can be reduced.

Although these known Tl--Ba--Ca--Cu--O system and Bi--Sr--Ca--Cu--O system oxide superconductors show very high Tco's at which the superconducting property is observed, their Tci's at which the apparent electrical resistance become zero or undetectable are such low as about 80 to 90 K. which is not so different from that of the Y₁ Ba₂ Cu₃ O_(7-x) system because these compound oxide superconductors contain several different phases. Still more, their critical current density values (Jc) are inferior to that of the Y₁ Ba₂ Cu₃ O_(7-x) system.

Still more, in the case of production of thallium type oxide superconductors, there is a special problem cause by such a fact that thallium is a very volatile element and toxic for human. In fact, it is difficult to obtain a thallium-containing oxide having a desired composition because the vapour pressure of thallium is relatively higher than the other elements. Further, the special attention must be paid to handle the material of the thallium-containing superconductor because thallium element is toxic for human.

An object of the present invention is to overcome the problems of the prior arts and to provide thallium-containing superconductors which is relatively easy to be obtained as a single phase and also which have improved superconducting properties and a method for producing the same.

SUMMARY OF THE INVENTION

The present invention provides a superconducting oxide material, characterized in that the superconducting oxide material contain compound oxide having a composition represented by the formula:

    (Tl.sub.(1-p-q) Bi.sub.p Pb.sub.q).sub.y γ.sub.z (α.sub.(1-r) β.sub.r).sub.s Cu.sub.v O.sub.w

in which each of "α" and "γ" is an element selected in IIa group of the periodic table, "β" is an element selected from a group comprising Na, K, Rb and Cs, "y", "z", "v", "w", "p", "q", "r" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦6.0, 1.0≦v, 5.0≦w, 0≦p≦1.0, 0≦q≦1.0, 0≦r≦1.0 and 0.5≦s≦3.0.

The expression "contain" means that the superconducting oxide material according to the present invention can contain additionally or inevitably the other compound oxides. In fact, a bulk oxide superconductor usually may consist of more than one phase. Therefore, all compound oxides containing the compound oxide defined by the present invention are included in the scope of the present invention.

The present invention provides also a process for preparing the superconducting oxide material, characterized by mixing oxide powders each containing Tl, Bi, Pb, an element α, an element β, an element γ and Cu in proportions of

    Tl:Bi:Pb:γ:α:β:Cu=h:i:j:k:l:m:n,

in which each of "α" and "γ" is an element selected in IIa group of the periodic table, "β" is an element selected from a group comprising Na, K, Rb and Cs, "h", "j", "k", "l", "m" and "n" are numbers each satisfying respective range of 0<h≦3.0, 0≦i<3.0, 0≦j<3.0, 0.5≦k≦6.0, 0≦l≦3.0 0≦m≦3.0 and 1.0≦n, and then sintering the resulting powder mixture at a temperature between 820° and 950° C. for 6 to 100 hours in oxygen gas atmosphere.

An essence of the present invention reside in that the oxide superconductor according to the present invention contain a compound oxide having a layered crystal structure of a tetragonal system which has one layer of Tl--O, (Tl, Pb)--O, (Tl, Bi)--O or (Tl, Pb, Bi)--O in the crystal.

Preferable compound oxides are represented by one of the following general formulas:

    (Tl.sub.(1-q) Pb.sub.q).sub.y γ.sub.z α.sub.s Cu.sub.v O.sub.w( 1)

in which each of "α" and "γ" is an element selected in IIa group of the periodic table, "y", "z", "v", "w", "q" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦6.0, 2.0≦v, 5.0≦w, 0≦q≦1.0 and 0.5≦s≦3.0, preferably 0<q≦0.5. This compound oxide has preferably such a crystal structure as having two to six layer of CuO corresponding to v=2 to 6.

    (Tl.sub.(1-p) Bi.sub.p).sub.y α.sub.s Ca.sub.z Cu.sub.v O.sub.w( 2)

in which "α" is Ba or Sr, "y", "z", "v", "w", "p" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦4.0, 1.0≦v≦5.0, 5.0≦w≦15.0, 0≦p≦1.0 and 0.5≦s≦3.0, preferably 0.2≦p≦0.8.

    (Tl.sub.(1-p-q) Bi.sub.p Pb.sub.q).sub.y α.sub.s Ca.sub.z Cu.sub.v O.sub.w                                                   ( 3)

in which "α" is Ba or Sr, "y", "z", "v", "w", "p", "q" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦4.5, 1.0≦v≦5.0, 5.0≦w≦15.0, 0≦p≦1.0, 0≦q≦0.6 and 0.5≦s≦3.0, preferably 0.2≦p≦0.8.

    Tl.sub.y Ca.sub.z (α.sub.(1-r) β.sub.r).sub.s Cu.sub.v O.sub.w( 4)

in which "α" is Ba or Sr, "β" is an element selected from a group comprising Na, K, Rb and Cs, "y", "z", "v", "w", "r" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦4.0, 2.0≦v≦5.0, 5.0≦w≦15.0, 0≦r≦0.8 and 0.5≦s≦3.0.

    (Tl.sub.(1-p-q) Bi.sub.p Pb.sub.q).sub.y Ca.sub.z (α.sub.(1-r) β.sub.r).sub.s Cu.sub.v O.sub.w                      ( 5)

in which "α" is Ba or Sr, "β" is an element selected from a group comprising Na, K, Rb and Cs, "y", "z", "v", "w", "p", "q", "r" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦4.0, 2.0≦v≦5.0, 5.0≦w≦15.0, 0≦p≦0.5, 0≦q≦0.5, 0≦r≦0.8 and 0.5≦s≦3.0.

The superconducting oxide material containing the above-mentioned compound oxide according to the present invention is preferably prepared by mixing one of oxide powders consisting of the following elements listed below with their proportions and then by sintering the resulting powder mixture at a temperature between 820° and 950° C. for 6 to 100 hours in oxygen gas atmosphere:

(1) Tl:Pb:Ca:Ba:Cu=h:j:k:l:n, in which 0<h<3.0, 0<j<3.0, 0.5≦k≦6.0, 0.5≦l≦3.0 and 2.0≦n,

(2) Tl:Bi:Ca:Ba:Cu=h:i:k:l:n, in which 0<h<3.0, 0<i<3.0, 0.5≦k≦6.0, 0.5≦l≦3.0 and 2.0≦n,

(3) Tl:Bi:Ca:Sr:Cu=h:i:k:l:n, in which 0<h<3.0, 0<i<3.0, 0.5≦k≦6.0, 0.5≦l≦3.0 and 2.0≦n,

(4) Tl:Bi:Pb:Ca:Sr:Cu=h:i:j:k:l:n, in which 0<h<3.0, 0≦i<3.0, 0≦j<3.0, 0.5≦k≦4.0, 0.5≦l≦3.0 and 1.0≦n≦5.0,

(5) Tl:Ca:α:β:Cu=h:k:l:m:n, in which "α" is Ba or Sr, "β" is an element selected from a group comprising Na, K, Rb and Cs and 0.5≦h≦3.0, 0.5≦k≦4.0, 0.1≦l≦3.0, 0≦m≦2.4 and 2.0≦n≦5.0, and

(6) Tl:Bi:Pb:Ca:α:β:Cu=h:i:j:k:l:m:n, in which "α" is Ba or Sr, "β" is an element selected from a group comprising Na, K, Rb and Cs and 0.5≦h<3.0, 0.5≦i<3.0, 0.5≦j<3.0, 0.5≦k≦4.0, 0.1≦l≦3.0, 0≦m≦2.4 and 2.0≦n≦5.0.

In operation, the material powder mixture is preferably wrapped with a metallic foil made of one of precious metals such as gold or their alloys. The sintering operation can be effected in an ordinary furnace. The interior of the furnace is preferably in the condition of oxygen-rich atmosphere. The oxygen gas is preferably fed continuously into the furnace during the sintering operation preferably at a rate of more than 0.1 liter per minute at 1 atm. Usual oxygen gas pressure is about 1 atm. but the sintering can be effected also at a higher oxygen pressure than 1 atm. According to the present invention, the sintering is effected at a temperature between 820° and 950° C. When the sintering temperature is not higher than 820° C., the resulting sintered mass becomes a mixture of different phases each having different critical temperature, so that the apparent Tc of the sintered mass become lower. To the contrary, if the sintering temperature is not lower than 950° C., the evaporation of thallium increase excessively so that it is difficult to adjust the composition of the sintered mass to desired atomic ratios and also it increases precipitates which doesn't contribute the superconductivity. The sintering can be effected for a time duration between 6 to 100 hours. When the sintering time is not longer than 6 hours, the material powder mixture is not sintered satisfactorily so that a desired superconductor can not be obtained. Longer sintering time than 100 hours may not effective to improve the superconducting property.

As is described hereinabove, the oxide superconductors according to the present invention exhibit very higher critical current density than the known oxide superconductors such as Bi--Sr--Ca--Cu--O system and Tl--Sr--Ca--Cu--O system while they exhibit the same or even higher critical temperature with respect to such known oxide superconductors. It is thought that such advantage might be obtained from such facts that the oxide superconducting materials according to the present invention have a novel layered crystal structure of tetragonal system having one layer of Tl--O, (Tl, Pb)--O, (Tl, Bi)--O or (Tl, Pb, Bi)--O and that the oxide superconducting materials according to the present invention are relatively easily obtained as a single phase.

BRIEF DESCRIPTION OF THE DRAWING

FIGS. 1 to 5 are X-ray diffraction charts of five oxide superconductors (Sample No. 1 to 5) obtained in Example 1 according to the present invention.

FIG. 6 is a X-ray diffraction chart of an oxide superconductor (Sample No. 6) obtained in Example 3 according to the present invention.

FIGS. 7 to 9 show respective temperature dependency of magnetic susceptibility of oxide superconductors (Sample No. 3 to 5) obtained in Example 1 according to the present invention.

FIG. 10 shows a temperature dependency of electric resistance of an oxide superconductor (Sample No. 1) obtained in Example 3 according to the present invention.

FIGS. 11 and 12 show respective temperature dependency of electric resistance and of magnetic susceptibility of an oxide superconductor (Sample No. 6) obtained in Example 3 according to the present invention.

Now, the present invention will be described in more details by examples, but the scope of the present invention should not be limited to the following special examples.

EXAMPLE 1

Oxide superconducting materials according to the present invention were prepared by the process according to the present invention. Powders of Tl₂ O₃, PbO, CaO, BaO₂ and CuO used as materials were mixed in such proportions that the atomic ratios of Tl:Pb:Ca:Ba:Cu in each sample became as followings:

(1) 0.8:0.2:3:1:3

(2) 0.75:0.25:3:1:3

(3) 0.8:0.2:3:1:3

(4) 0.95:0.05:3:1:3

(5) 0.95:0.05:3:1:3.

Then, each of the resulting powder mixture was compacted under a pressure of about 100 kg/cm² into a pellet. Each pellet was wrapped with a gold foil of 50 micron thick and was sintered at a fixed temperature selected from a range between 850° C. and 900° C. for about 10 hours in a furnace into which O₂ gas is flown at a rate of 200 ml/min to obtain an oxide superconductor according to the present invention.

The powder mixture of Sample No. 4 and 5 had the same atomic ratios but they were sintered at different sintering temperature of 870° C. (sample No. 4) and 850° C. (sample No. 5) respectively.

All of the resulting oxide superconductors were found that they contained compound oxide represented by the general formula:

    (Tl.sub.(1-q) Pb.sub.q).sub.y Ca.sub.z Ba.sub.s Cu.sub.v O.sub.w

in which "y", "z", "v", "w", "q" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦6.0, 2.0≦v, 5.0≦w, 0≦q≦1.0 and 0.5≦s≦3.0.

Table.1 shows the properties of each oxide superconducting material obtained and FIGS. 1 to 5 show X-ray diffraction data thereof. FIGS. 7 to 9 show the result of magnetic susceptibility measured on the samples No. 3, 4 and 5 respectively. In the composition shown in Table 1, there are such cases that the ratio of Tl to Pb and the ratio of Ca to Cu don't coincide with the theoretical values which are expected by the analysis of crystal structure because the values shown in Table 1 are measured values and conain a tolerance.

For a comparison, the coresponding properties of known superconducting materials represented by Tl₂ Ca₂ Ba₂ Cu₃ O₁₀ and (Bi, Pb)₂ Ca₂ Sr₂ Cu₃ O₁₀ are also shown in Table 1.

From the Table 1, it is apparent that the oxide superconducting material according to the present invention show higher critical current density Jc than the known oxide superconducting materials while same or even higher critical temperature Tc is observed.

                                      TABLE 1                                      __________________________________________________________________________     sample              lattice  Tci Jc                                            No   composition    constant (K) (A/cm.sup.2)                                  __________________________________________________________________________     1    (Tl, Pb).sub.1 Ca.sub.1 Ba.sub.2 Cu.sub.2 O.sub.7                                             a =                                                                                3.86 Å                                                                           80 400                                                               c =                                                                               12.95 Å                                             2    (Tl, Pb).sub.1 Ca.sub.2 Ba.sub.2 Cu.sub.3 O.sub.9                                             a =                                                                                3.86 Å                                                                          102 410                                                               c =                                                                               16.11 Å                                             3    Tl.sub.0.80 Pb.sub.0.20 Ca.sub.3.0 Ba.sub.2.0 Cu.sub.3.9 O.sub.x                              a =                                                                                3.85 Å                                                                          121 520                                                               c =                                                                               19.36 Å                                             4    Tl.sub.0.82 Pb.sub.0.15 Ca.sub.4.0 Ba.sub.2.0 Cu.sub.4.9 O.sub.y                              a =                                                                                3.85 Å                                                                          113 470                                                               c =                                                                               22.22 Å                                             5    Tl.sub.0.90 Pb.sub.0.16 Ca.sub.5.0 Ba.sub.2.0 Cu.sub.5.8 O.sub.z                              a =                                                                                3.85 Å                                                                          102 --                                                                c =                                                                               25.97 Å                                             Comparative                                                                    Tl.sub.2 Ca.sub.2 Ba.sub.2 Cu.sub.3 O.sub.10                                                                118 270                                           (Bi, Pb).sub.2 Ca.sub.2 Sr.sub.2 Cu.sub.3 O.sub.10                                                          108 255                                           __________________________________________________________________________

EXAMPLE 2

Oxide superconducting materials according to the present invention were prepared by the process according to the present invention. Powders of Tl₂ O₃, Bi₂ O₃, BaO₂, CaO and CuO (purity is higher than 99.9%) used as materials were weighted and mixed in the proportions shown in Table 2 to prepare two samples of powder mixture. Then, the resulting powder mixtures were compacted into pellets. the resulting each pellet was wrapped with a gold foil and was sintered at a temperature of 870° C. for 12 hours.

The resulting two samples of oxide superconductors were found that they contained compound oxide represented by the general formula:

    (Tl.sub.(1-p) Bi.sub.p).sub.y Ba.sub.s Ca.sub.z Cu.sub.v O.sub.w

in which "y", "z", "v", "w", "p" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦4.0, 1.0≦v≦5.0, 5≦w≦15.0, 0≦p≦1.0 and 0.5≦s≦3.0.

On the resulting oxide superconductors, the critical temperature and the critical current density at liquid nitrogen temperature were measured and X-ray diffraction charts were obtained in order to check phases produced.

For a comparison, a comparative superconducting material was prepared by sintering a powder mixture containing solely of Tl₂ O₃, BaO₂, CaO and CuO and the superconducting properties were determined by the same method as above.

Table 2 shows the ratios of elements in the material powder mixture, the superconducting properties and the crystal structure (phase) determined by X-ray diffraction analysis including the value "y" in the general formula.

From the Table 2, it is apparent that the oxide superconducting material according to the present invention show much higher critical current density Jc than the known oxide superconducting material while same or even higher critical temperature Tc is observed.

                                      TABLE 2                                      __________________________________________________________________________            Composition of                                                                 the powder mixture      Tci                                                                               Jc                                                  Tl Bi                                                                               Ba Ca                                                                               Cu Phase obtained                                                                          y (K)                                                                               (A/cm.sup.2)                                 __________________________________________________________________________     Example                                                                               1.4                                                                               0.6                                                                              2  2 3  a = 3.85 Å                                                                          2 110                                                                               400                                                              c = 15.8 Å                                                                 tetragonal system                                                 1.6                                                                               0.4                                                                              2  2 3  same as above                                                                           2 115                                                                               450                                          Comparative                                                                           2  --                                                                               2  2 3  a = 3.85 Å                                                                          --                                                                               112                                                                               270                                                              c = 35.8 Å                                             __________________________________________________________________________      Note: Tci is a temperature where perfect zero resistance was observed    

EXAMPLE 3

A plurality of oxide superconducting materials according to the present invention were prepared by the process according to the present invention. Powders of Tl₂ O₃, Bi₂ O₃, PbO, CaO, SrO and CuO (purity is higher than 99.9%) used as materials were weighted and mixed in the proportions shown in Table 3, Table 4 and Table 5 to prepare powder mixture samples. Then, the resulting powder mixture samples were compacted into pellets. The resulting each pellet was wrapped with a gold foil and was sintered at a temperature of 870° C. for 12 hours.

All of the resulting oxide superconductors were found that they contained compound oxide represented by the general formula:

    (Tl.sub.(1-p) Bi.sub.p).sub.y Sr.sub.s Ca.sub.z Cu.sub.v O.sub.w

in which "y", "z", "v", "w", "p" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦4.0, 1.0≦v≦5.0, 5≦w≦15.0, 0≦p≦1.0 and 0.5≦s≦3.0,

or compound oxide represented by the general formula:

    (Tl.sub.(1-p-q) Bi.sub.p Pb.sub.q).sub.y Sr.sub.s Ca.sub.z Cu.sub.v O.sub.w

in which "y", "z", "v" "w" "p" "q" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦4.5, 1.0≦v≦5.0, 5.0≦w≦15.0, 0≦p≦1.0, 0≦q≦0.6 and 0.5≦s≦3.0.

On the resulting oxide superconductors, the critical temperature and the critical current density at liquid nitrogen temperature were measured and X-ray diffraction charts were obtained in order to check phases produced. The value "y" in the general formula was also determined in several samples.

From these experimental data, it was confirmed that a novel layered crystal structure of a tetragonal system having a mixed layer of Tl and Bi or a mixed layer of Tl and Pb was produced in the resulting oxide superconductor. From the analysis of the proportion of the phase obtained by X-ray diffraction chart, it was concluded that this novel phase contributes to a superconducting phase.

For a comparison, the same test as above was repeated for comparative superconducting materials which were prepared by sintering a powder mixture containing solely of Bi₂ O₃, SrO, CaO and CuO and a powder mixture containing solely of Bi₂ O₃, SrO, CaO, CuO and PbO.

The ratios in the material powder mixture and the results of tests are also summarized in Table 3, 4 and 5. FIG. 10 shows a temperature dependency of electric resistance measured on the sample No. 1. FIG. 6 shows a X-ray diffraction chart obtained from the sample No. 6. FIGS. 11 and 12 show a temperature dependency of magnetic susceptibility and a temperature dependency of electric resistance obtained from the sample No. 6 respectively.

All of the oxide superconducting materials according to the present invention show much higher critical current density Jc than the known oxide superconducting material while same or even higher critical temperature Tc is observed.

                  TABLE 3(1)                                                       ______________________________________                                                Composition of                                                          Sample the powder mixture    Tci    Jc                                         No     Tl     Bi     Pb   Sr   Ca   Cu   (K)  (A/cm.sup.2)                     ______________________________________                                         Example                                                                        (1)    0.8    0.2    --   2    2    3    115  900                              (2)    0.7    0.3    --   2    2    3    100  450                              (3)    0.6    0.4    --   2    2    3    105  550                              (4)    0.4    0.6    --   2    2    3    100  500                              (5)    0.2    0.8    --   2    2    3     98  400                              (6)    1      1      --   2    2    3    105  780                              (7)    0.6    0.3    0.1  2    2    3    108  650                              (8)     0.56   0.24  0.2  2    2    3    110  700                              (9)     0.42   0.18  0.4  2    2    3    113  750                              (10)    0.35   0.15  0.5  2    2    3    110  680                              (11)    0.28   0.12  0.6  2    2    3    108  650                              (12)    0.21   0.09  0.7  2    2    3     80   90                              ______________________________________                                          Note: Tci is a temperature where perfect zero resistance was observed. Th      phase obtained was a tetragonal system having the lattice constant of a =      3.8 Å and c = 15.3 Å in all samples prepared.                    

                  TABLE 3(2)                                                       ______________________________________                                                  Composition of                                                        Sample   the powder mixture  Tci    Jc                                         No       Tl     Bi     Pb  Sr   Ca  Cu   (K)  (A/cm.sup.2)                     ______________________________________                                         Comparative                                                                    Example I                                                                      (13)       0.9  0.1    --  2    2   3    78    10                              (14)       0.1  0.9    --  2    2   3    80   100                              (15)     0      2      --  2    2   3    80    90                              (16)     1      0      --  2    2   3    75   --                               (17)     0      1.6    0.4 2    2   3    103  120                              ______________________________________                                          Note: Tci is a temperature where perfect zero resistance was observed    

                  TABLE 4                                                          ______________________________________                                                  Composition of                                                        Sample   the powder mixture  Tci    Jc                                         No       Tl     Bi    Pb   Sr  Ca   Cu   (K)  (A/cm.sup.2)                     ______________________________________                                         Example                                                                        II                                                                             (18)     0.7    0.3   --   2   1    2    86   120                              (19)     0.6    0.4   --   2   1    2    90   150                              (20)     0.4    0.6   --   2   1    2    85   120                              (21)     0.2    0.8   --   2   1    2    85   120                              (22)     0.6    0.3   0.1  2   1    2    95   300                              Comparative                                                                    Example II                                                                     (23)     0.9    0.1   --   2   1    2    78    10                              (24)     0.1    0.9   --   2   1    2    78    20                              (25)     0      2     --   2   1    2    78    20                              (26)     1      0     --   2   1    2    75   --                               (27)     0      1.6   0.4  2   1    2    90   180                              ______________________________________                                          Note: Tci is a temperature where perfect zero resistance was observed    

                                      TABLE 5                                      __________________________________________________________________________            Composition of Lattice                                                  Sample the powder mixture                                                                            constant Tci                                                                               Jc                                           No     Bi Tl                                                                               Pb Sr                                                                               Ca Cu                                                                               (Å)                                                                              y  (K)                                                                               (A/cm.sup.2)                                 __________________________________________________________________________     Example                                                                        III                                                                            (28)   1.2                                                                               0.8                                                                              -- 2 2  3 a = 3.8                                                                              2  100                                                                               450                                                                c = 15.3                                                                       tetragonal                                               (29)   0.8                                                                               1.2                                                                              -- 2 2  3 a = 3.8                                                                              2  105                                                                               550                                                                c = 15.3                                                                       tetragonal                                               (30)   1.0                                                                               0.6                                                                              0.4                                                                               2 2  3 a = 3.8                                                                              2  110                                                                               500                                                                c = 15.8                                                 Comparative                                                                    Example III                                                                    (31)   2  --                                                                               -- 2 2  3 a = 5.41                                                                             --  78                                                                                10                                                                c = 36.8                                                                       a = 5.41                                                                       c = 30.6                                                 (32)   1.6                                                                               0.4                                                                              -- 2 2  3 a = 5.41                                                                             -- 103                                                                               120                                                                c = 36.8                                                 __________________________________________________________________________      Note: Tci is a temperature where perfect zero resistance was observed    

EXAMPLE 4

Oxide superconducting materials according to the present invention were prepared by the process according to the present invention. Powders of Tl₂ O₃, CaO, BaO₂, Cs₂ CO₃ and CuO (purity is higher than 99.9%) used as materials were weighted and mixed in the proportions shown in Table 6 to prepare five samples of powder mixture. Then, the resulting powder mixtures were compacted into pellets. The resulting each pellet was wrapped with a gold foil and was sintered at a temperature of 850° C. for 12 hours in oxygen gas stream. For a comparison, a comparative superconducting material was prepared by sintering a powder mixture containing the same materials except Cs₂ CO₃.

The resulting all samples of oxide superconductors were found that they contained compound oxide represented by the general formula:

    Tl.sub.y Ca.sub.z (Ba.sub.(1-r) Cs.sub.r).sub.s Cu.sub.v O.sub.w

in which "y", "z", "v", "w", "r" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦4.0, 2.0≦v≦5.0, 5.0≦w≦15.0, 0≦r≦0.8 and 0.5≦s≦3.0.

On the resulting oxide superconductors, the critical temperature Tc and the critical current density Jc at liquid nitrogen temperature were measured. The results are summarized in Table 6.

All of the oxide superconducting materials according to the present invention show much higher critical current density Jc than known oxide superconducting material while same or even higher critical temperature Tc is observed.

                  TABLE 6                                                          ______________________________________                                                  Composition of                                                        Sample   the powder mixture  Tci    Jc                                         No       TI     Ca     Ba   Cs    Cu   (K)  (A/cm.sup.2)                       ______________________________________                                         Comparative                                                                             2      2      2.0  --    3    110  300                                (1)      2      2       1.95                                                                                0.05 3    113  280                                (2)      2      2      1.8  0.2   3    116  350                                (3)      2      2      1.0  1.0   3    116  400                                (4)      2      2      0.4  1.6   3    117  450                                (5)      2      2      0.2  1.8   3    --*  --*                                ______________________________________                                          Note: * no superconductor above 4.2 K.                                   

EXAMPLE 5

Oxide superconducting materials according to the present invention were prepared by the same process as Example 4 except that Bi₂ O₃ and PbO were added additionally. The resulting oxide superconductor was evaluated by the same method as Example 4. Table 7 shows the composition of the material powder and the properties of the resulting oxide superconductor.

The resulting oxide superconducting material was found that it contained compound oxide represented by the general formula:

    (Tl.sub.(1-p-q) Bi.sub.p Pb.sub.q).sub.y Ca.sub.z (Ba.sub.(1-r) Cs.sub.r).sub.s Cu.sub.v O.sub.w

in which "y", "z", "v", "w", "p", "q", "r" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦4.0, 2.0≦v≦5.0, 5.0≦w≦15.0, 0≦p≦0.5, 0≦q≦0.5, 0≦r≦0.8 and 0.5≦s≦3.0.

This oxide superconducting material according to the present invention shows much higher critical current density Jc than known oxide superconducting material while same or even higher critical temperature Tc is observed.

                  TABLE 7                                                          ______________________________________                                               Composition of                                                           Sample                                                                               the powder mixture     Tci    Jc                                         No    Tl     Bi     Pb  Ca   Ba  Cs   Cu   (K)  (A/cm.sup.2)                   ______________________________________                                         (6)   1.6    0.2    0.2 2    1   1    3    116  350                            ______________________________________                                    

EXAMPLE 6

Oxide superconducting materials according to the present invention were prepared by the same process as Example 4 except that BaO₂ is replaced by SrO₂. The resulting oxide superconductor was evaluated by the same method as Example 4. Table. 8 shows the composition of the material powder and the properties of the resulting oxide superconductor.

All of the resulting oxide superconducting materials were found that they contained compound oxide represented by the general formula:

    Tl.sub.y Ca.sub.z (Sr.sub.(1-r) Cs.sub.r).sub.s Cu.sub.v O.sub.w

in which "y", "z", "v", "w", "r" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦4.0, 2.0≦v≦5.0, 5.0≦w≦15.0, 0≦r≦0.8 and 0.5≦s≦3.0.

These oxide superconducting materials according to the present invention show much higher critical current density Jc than known oxide superconducting material while same or even higher critical temperature Tc is observed.

                  TABLE 8                                                          ______________________________________                                                  Composition of                                                        Sample   the powder mixture  Tci    Jc                                         No       Tl     Ca     Sr   Cs    Cu   (K)  (A/cm.sup.2)                       ______________________________________                                         Comparative                                                                             2      2      2.0  --    3     70  --                                 (7)      2      2       1.95                                                                                0.05 3     72  --                                 (8)      2      2      1.8  0.2   3    100  280                                (9)      2      2      1.0  1.0   3    105  400                                (10)     2      2      0.4  1.6   3    103  350                                (11)     2      2      0.2  1.8   3    --*  --*                                ______________________________________                                          NB: * no superconductor above 4.2 K.                                     

EXAMPLE 7

Oxide superconducting material according to the present invention was prepared by the same process as Example 6 except that Bi₂ O₃ and PbO were added additionally. The resulting oxide superconductor was evaluated by the same method as Example 6. Table. 9 shows the composition of the material powder and the properties of the resulting oxide superconductor.

The resulting oxide superconducting material was found that it contained compound oxide represented by the general formula:

    (Tl.sub.(1-p-q) Bi.sub.p Pb.sub.q).sub.y Ca.sub.z (Sr.sub.(1-r) Cs.sub.r).sub.s Cu.sub.v O.sub.w

in which "y", "z", "v", "w", "p", "q", "r" and "s" are numbers each satisfying respective range of 0.5≦y≦3.0, 0.5≦z≦4.0, 2.0≦v≦5.0, 5.0≦w≦15.0, 0≦p≦0.5, 0≦q≦0.5, 0≦r≦0.8 and 0.5≦s≦3.0.

The oxide superconducting material according to the present invention show much higher critical current density Jc than known oxide superconducting material while same or even higher critical temperature Tc is observed.

                  TABLE 9                                                          ______________________________________                                               Composition of                                                           Sample                                                                               the powder mixture     Tci    Jc                                         No    Tl     Bi    Pb   Ca   Sr   Cs  Cu   (K)  (A/cm.sup.2)                   ______________________________________                                         (12)  1.6    0.2   0.2  2    1    1   3    108  380                            ______________________________________                                     

We claim:
 1. Superconducting compound oxide represented by the general formula (II):

    (Tl.sub.(1-p-q) Bi.sub.p Pb.sub.q)Sr.sub.2 Ca.sub.2 Cu.sub.3 O.sub.w(II)

in which small letters w, p, and q are numbers each satisfying respective ranges of 5.0≦w, 0.12≦p≦0.3, and 0.1≦q≦0.6. 